SBS - The best value in QMS software

How to Identify and Evaluate Environmental Aspects and Impacts

Randy

Super Moderator
#51
I have met a couple of good ones as well (to help even out the scorecard).

In particular the witness auditor that has audited me a couple of times in a course I deliver is excellant and I feel perfectly comfortable with the process and results. Feedback is excellant and the findings are supported by good evidence. This particular auditor would be an asset to any organization.
 
Elsmar Forum Sponsor

Helmut Jilling

Auditor / Consultant
#52
Randy said:
I have met a couple of good ones as well (to help even out the scorecard).

In particular the witness auditor that has audited me a couple of times in a course I deliver is excellant and I feel perfectly comfortable with the process and results. Feedback is excellant and the findings are supported by good evidence. This particular auditor would be an asset to any organization.

The ones I've had were generally good as well. I just wish they would clean their own house first.
 
T

tarheels4 - 2007

#53
hjilling said:
You know, it is frustrating. In the last few weeks I have personally spent thousands of dollars getting training and testing so I can renew my TS credentials. It probably cost $5000 plus, if I factor in the lost audit days as well.

Each year, I spend several thousand to renew or retrain in one standard or another...just so some clod like that can witness me, and verify whether I am competent. Because they want to improve the integrity of the programs.

You would think they could do a better job policing themselves.
I think one way to look at it is that the relationship of the AB to the CB is like that of the CB to the organization audited. The auditor is the one one who is usually shi t on.

As you said earlier, during a AB witness audit the auditor may be "nitpicked" to death, the easy scapegoat (the CB is the customer of the AB); and on the the other hand (organization is the customer of the CB), the CB in most cases I bet, would support the customer rather than the auditor, if there was an appeal. The auditor is much easier to replace, and besides, the revenue comes from the organization (customer).
 
Last edited by a moderator:
Q

QMarc

#54
Right ...!

Good morning covers,

interesting discussion to my last post here :)

Well, I agree with Randys standard opinion: Please choose the tools best fitting to your company ... right?! What we do for audits and auditors is something that fits to meet the standard requirements for 14K certification.

So it may happen that there will be discrepancies in between the two ways. In manners of a small and effective documentation this is wasting work and time.

My question to this problem is ... who is writing the standards and who ist setting the practical standards in daily work ... and there I find some discrepancies too.

@hjilling: You may be right with your opinion, but in our company all workers are well trained and the management employees are forced by the CEO to consider all aspects and impacts during their work. So for them a documented procedure or table or something else is nothing they have a look to. Even it is not a strategic tool for the management team.
Furthermore 20 % of the employees are loosing their job in the next months ... might be an argument for documentation, isn´t it?

QMarc
 
E

Enviroken

#55
Back to what people were writing earlier about orgnisations not committing to ISO 14001 just getting the paper and thats it. Have any of you actually refused certidication due to witnessing this when peforming an audit? I recently asked an auditor from a large professional organisation this same question but he managed to talk for ages in response but not answer the question!

So much for top management commitment in those previous examples!!!
 

Paul Simpson

Trusted Information Resource
#57
Yes

Enviroken said:
Have any of you actually refused certidication due to witnessing this when peforming an audit?
Yes. Without giving any details away - client confidentiality. I worked as a contract auditor for a certification body and audited this company. They had written their aspects list around what they thought they would do in the operational control area and had identified around 30% of the aspects that I could see with their processes. That - together with a few other glaring issues in environmental planning added up to a major.
 

Helmut Jilling

Auditor / Consultant
#58
QMarc said:
...in our company all workers are well trained and the management employees are forced by the CEO to consider all aspects and impacts during their work. So for them a documented procedure or table or something else is nothing they have a look to. Even it is not a strategic tool for the management team. QMarc

Perhaps, I am misunderstanding. But, if everyone considers all the Aspects and Impacts like the CEO requires, then it should only take 30-60 minutes to jot it down onto a table of some sort.

Perhaps, the greater likelihood is the American expression "out of sight ... out of mind." Meaning, if it is not documented in a form that can be reviewed and analyzed, there is a greater likelihood it is not analyzed as well.

There is another famous quote that says, "To improve it, you must measure it (and manage it)."
 

Helmut Jilling

Auditor / Consultant
#59
Paul Simpson said:
Yes. Without giving any details away - client confidentiality. I worked as a contract auditor for a certification body and audited this company. They had written their aspects list around what they thought they would do in the operational control area and had identified around 30% of the aspects that I could see with their processes. That - together with a few other glaring issues in environmental planning added up to a major.

That sounds appropriate, particularly if there was evidence they did not put good effort or thought into it. (see, we're back in our usual role of agreeing with each other...:D )
 
Q

QMarc

#60
hjilling said:
Perhaps, I am misunderstanding. But, if everyone considers all the Aspects and Impacts like the CEO requires, then it should only take 30-60 minutes to jot it down onto a table of some sort.
Yeah, you are right ... the table is not the problem. The auditor wanted us to use it as an strategic instrument and that´s not the way it is used.

It is still a document which mirrors the same important Aspects and Impacts considered in daily work, but that´s all.

Let me give you an example. Waste amounts are summarized and discussed for reduction more or less once a year. Everybody knows the aim to reduce the waste amounts.
So waste amount is an important topic for us, and why should we demonstrate it in another way by use of a table?

My aim to post it here, was to get an impression, if somebody has a mechanism to get more benefit of it ... can we?

QMarc
 
Thread starter Similar threads Forum Replies Date
R Identify Medical Device characterstics as Annex C of ISO 14971 Risk Management ISO 14971 - Medical Device Risk Management 5
T ISO 9001 8.5.2. - Identification and traceability to Identify Outputs - Services ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
U When do we identify Residual Risk? Risk Management Principles and Generic Guidelines 11
D How to Identify the Risks and Opportunities required for QMS Processes? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
D How to identify and confirm that the developed device fall under Israel electro medical device category Other Medical Device Regulations World-Wide 0
D How to identify and confirm that the developed device fall under Israel electro medical device category Other Medical Device Regulations World-Wide 1
E How do you identify what standards a country recognizes outside of FDA, EU, Health Canada Other Medical Device Related Standards 1
Marc Can you identify this moth? 19 January 2019 After Work and Weekend Discussion Topics 6
K Please help identify appropriate statistical treatment Statistical Analysis Tools, Techniques and SPC 13
D Help identify a Nationally Recognized Testing Laboratory (NRTL) (UL) certified lab General Measurement Device and Calibration Topics 3
T To Identify the Applicable MDD Directive - Prepared blood smear EU Medical Device Regulations 13
A Requirement to Identify Changes to record in ISO 13485 : 2016 ISO 13485:2016 - Medical Device Quality Management Systems 4
R AS9100D Cl. 8.4.2 - Identify Raw Material as a Significant Operational Risk AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
C How to Identify Counterfeit Medications (drugs)? US Food and Drug Administration (FDA) 5
P How to identify the Management Representative ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
T How to identify requirements for 'Incoming inspection' Inspection, Prints (Drawings), Testing, Sampling and Related Topics 5
M How to identify software configuration items in a BOM Quality Manager and Management Related Issues 3
S Resource Planning/How to identify IATF 16949 - Automotive Quality Systems Standard 1
V How to identify Customer Specific Requirement If is not provided by Customer Customer and Company Specific Requirements 5
B How to identify Six Sigma Yellow Belt Project Six Sigma 4
C Must we identify steps taken to identify the Root Cause of a failure Nonconformance and Corrective Action 15
G How to identify Key Characteristics (KC) in a Design FMEA (DFMEA) FMEA and Control Plans 2
X Existing Toolroom Process Validation - Need to identify clauses addressed. Manufacturing and Related Processes 7
C How Can I Identify 304 Stainless Steel? Manufacturing and Related Processes 6
Geoff Cotton How to identify Stakeholders in a Company Quality Tools, Improvement and Analysis 9
M How to identify CTQ / Critical Characteristics using the DFMEA approach. FMEA and Control Plans 3
R 3rd Party Audit Comment - Identify ISO Clauses/Sub Clauses to each Process Quality Management System (QMS) Manuals 45
J AS9100:C Risk Management - Identify the Risk for the Sales/Contract Processes AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 12
T How to Identify Taper Gages without potentially damaging them General Measurement Device and Calibration Topics 5
N How to Number (Identify) and Index Forms Document Control Systems, Procedures, Forms and Templates 1
A DoC for Software Product - How can I identify the specific units that are covered? EU Medical Device Regulations 6
T How to Identify "Observation" in Internal Audits? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 26
X Audit Findings - The Process/Clause Matrix does not identify all the processes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 30
S Identify Environment Aspect by Activities Approach ISO 14001:2015 Specific Discussions 4
T Can't identify my company's "Key Process" Process Maps, Process Mapping and Turtle Diagrams 27
B Effectiveness of 200% Visual Inspection to Identify Defects and Defectives Inspection, Prints (Drawings), Testing, Sampling and Related Topics 32
N Definition IDENTIFY and DETERMINE - What is the technical difference between the words Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 64
A Procedure to Identify Potential Emergency Situations and Accidents Miscellaneous Environmental Standards and EMS Related Discussions 4
D AS9102 - How to title the attached form and how to identify the characteristics AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
kedarg6500 How to Identify Critical to Quality Characteristics (CTQ) FMEA and Control Plans 2
Le Chiffre At what point do you need to identify a U.S. Agent - 510(k) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
M New to AS9100 - Clause 7.5.3 - Do you have to identify each part produced AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
S Form to identify status of product on the production floor. IATF 16949 - Automotive Quality Systems Standard 5
L Special Characteristics - What if the customer does not identify any SCs? FMEA and Control Plans 5
M How do you identify the wrong orientation in complex wiring harness? Manufacturing and Related Processes 21
W How do you address clause 4.1 General requirements - Identify the processes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 21
S CE Mark using Registered Trademark to identify the legal manufacturer EU Medical Device Regulations 6
B Determine vs. identify (as in clause 4.1 a), any differences? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
B How to identify the processes needed for quality management system ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
I Skill Matrix Format as a Tool to Identify Training Needs Document Control Systems, Procedures, Forms and Templates 1

Similar threads

Top Bottom